Team:Jilin China/Outline

From 2014.igem.org

(Difference between revisions)
Line 208: Line 208:
<li>Data query and project theme select </li>
<li>Data query and project theme select </li>
<li>Experiment scheme design </li>
<li>Experiment scheme design </li>
-
<li>Codon optimization of MlrA gene by lactic acid bacteria codons）</li>
+
<li>Codon optimization of MlrA gene by Lactococcus lactis codons）</li>
<li>MlrA gene sequence design and split</li>
<li>MlrA gene sequence design and split</li>
<li>RFP-Mlr-GFP sequence design and split</li></ol>
<li>RFP-Mlr-GFP sequence design and split</li></ol>
Line 223: Line 223:
<ol>
<ol>
<li>construction of the recombinant vector pMG-mlr</li>
<li>construction of the recombinant vector pMG-mlr</li>
-
<li>construction of the recombinant vector pMG-mlr</li>
+
<li>Recombinant vector was transformed into Escherichia coli</li>
-
<li>Synthetic primer by company (33 pieces in total)</li>
+
<li>GFP-mlrA expression by mlr promoter and detection in Escherichia coli</li>
-
<li>Repeat PCR for many times, recovery them and then get the complete gene product</li>
+
<li>Detection of microcystins LR degradation ability in water by Recombinant Escherichia coli</li></ol>
-
<li>Sub cloning vector and sequenced</li>
+
<h2>September, 2014</h2>
-
<li>Try to express by E.coli and analyze the effect of this protein</li>
+
<ol>
-
<li>Express by lactic acid bacteria</li></ol>
+
<li>Recombinant vector was transformed into Lactococcus lactis</li>
-
<h2>July to Sept, 2014</h2>
+
<li>GFP-mlrA expression by mlr promoter and detection in Lactococcus lactis</li>
 +
<li>Detection of microcystins LR degradation ability in water by Recombinant Lactococcus lactis</li></ol>
 +
<h2>October, 2014</h2>
<ol>
<ol>
-
<li>Discussion about many possible paths include MC-LR</li>
+
<li>Detection of microcystins LR degradation ability in the natural environment by Recombinant Escherichia coli</li>
-
<li>Try cloning Pseudomonas  natural promoter.(non-coding sequences in Mlr enzyme series )</li>
+
<li>Detection of microcystins LR degradation ability in the natural environment by Recombinant Lactococcus lactis</li>
-
<li>Synthesis by pieces then got complete product.</li>
+
 
-
<li>The gene transformed into E.coli and verify its functions.</li>
+
-
<li>Transform this gene by many ways into lactic acid bacteria and verify the function of promoter.</li></ol>
+
</div>
</div>

Revision as of 03:26, 18 October 2014

Welcome!
Team Jilin_China

May, 2014

  1. Data query and project theme select
  2. Experiment scheme design
  3. Codon optimization of MlrA gene by Lactococcus lactis codons）
  4. MlrA gene sequence design and split
  5. RFP-Mlr-GFP sequence design and split

June, 2014

  1. MlrA gene synthesis and sequence
  2. RFP-Mlr-GFP gene synthesis and sequence

July, 2014

  1. MlrA gene expression and detection
  2. RFP-Mlr-GFP gene expression and detection
  3. Screening of microcystin LR sensitive promoter

August, 2014

  1. construction of the recombinant vector pMG-mlr
  2. Recombinant vector was transformed into Escherichia coli
  3. GFP-mlrA expression by mlr promoter and detection in Escherichia coli
  4. Detection of microcystins LR degradation ability in water by Recombinant Escherichia coli

September, 2014

  1. Recombinant vector was transformed into Lactococcus lactis
  2. GFP-mlrA expression by mlr promoter and detection in Lactococcus lactis
  3. Detection of microcystins LR degradation ability in water by Recombinant Lactococcus lactis

October, 2014

  1. Detection of microcystins LR degradation ability in the natural environment by Recombinant Escherichia coli
  2. Detection of microcystins LR degradation ability in the natural environment by Recombinant Lactococcus lactis

Retrieved from "http://2014.igem.org/Team:Jilin_China/Outline"